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Mumie sirop na travah (Syrup) Instructions for Use

Marketing Authorization Holder

Pharmgroup, LLC (Russia)

Contact Information

PHARMGROUP LLC (Dietary Supplement) (Russia)

Dosage Form

Bottle OTC Icon Mumie sirop na travah Syrup: bottle 100 ml, 200 ml, or 250 ml

Dosage Form, Packaging, and Product Composition

Composition Altai mumiyo, greater burdock root, stinging nettle leaves, marsh cinquefoil herb, elecampane root, citric acid, sodium benzoate, sugar, ascorbic acid, drinking water.

Content of biologically active substances per 100 ml Vitamin C – 300 mg, flavonoids in terms of rutin not less than 2 mg, tannins in terms of tannin not less than – 0.25%, inulin not less than – 1.3%, humic acids – 1%.

Dosage form and packaging
Syrup. In 100 ml, 200 ml, or 250 ml bottles.

Therapeutic Category

Dietary supplement for supporting the function of the musculoskeletal system

Scope of Application

Of the Mumie sirop na travah product

Recommended as a dietary supplement – a source of tannins, an additional source of vitamin C, containing humic acids.

Indications

  • Use as a dietary supplement to provide supplemental nutrients.
  • Use as a source of tannins and humic acids.
  • Use as an additional source of vitamin C for general nutritional support.

This product is recommended for supporting the normal function of the musculoskeletal system as part of a dietary regimen.

ICD codes

ICD-10 code Indication
E63.8 Other specified types of nutritional deficiency
ICD-11 code Indication
5B7Z Malnutrition, unspecified
8D40.0 Encephalopathy due to nutritional deficiency

Dosage Regimen

The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen.

Take orally. For adults, administer one dessert spoon (10 ml) three times daily with meals.

Mix the dose into tea, mineral water, or another beverage prior to ingestion. Continue the course of intake for a period of two to three weeks.

This product is not a medicine. Do not exceed the recommended daily dosage.

Adverse Reactions

Adverse reactions are possible, primarily in individuals with hypersensitivity to any product component.

Observe for signs of allergic reactions, including skin rash, itching, or urticaria. Discontinue use immediately if any adverse effects occur and seek medical advice.

Drug Interactions

No specific drug interactions are currently known for this dietary supplement.

Concurrent use with prescription medications warrants caution. Consult a healthcare professional before combining this product with any other drugs.

Contraindications

  • Do not use if you have a known hypersensitivity or individual intolerance to any of the components.
  • Do not use during pregnancy or while breastfeeding.
  • Do not use if you have diabetes mellitus due to the sugar content.

Consult a physician prior to initiating use to assess suitability and rule out potential contraindications.

Overdose

Exceeding the recommended dose may increase the risk of adverse effects.

Symptoms of overdose are not well documented but may include gastrointestinal discomfort or manifestations of hypervitaminosis C, such as nausea or diarrhea.

In case of significant overdose, seek medical attention and discontinue use. Treatment should be symptomatic and supportive.

Dispensing Status

Sold to the public through pharmacy networks and specialized stores, departments of the retail network.

Storage Conditions

Store in a dry place, protected from light, at a temperature not exceeding 25°C (77°F).

Shelf Life

Shelf life – 2 years.

Important Safety Information

This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.

Medical Disclaimer

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